Canonical Allele Identifier: CA2648156907
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465537del , CM000663.2:g.154465537del GRCh38
NC_000001.10:g.154438013del , CM000663.1:g.154438013del GRCh37
NC_000001.9:g.152704637del NCBI36
NG_012087.1:g.65345del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*157del MANE Select ENSP00000357470.3:n.*157del
ENST00000344086.8:c.*372del ENSP00000340589.4:n.*372del
ENST00000368485.7:c.*157del ENSP00000357470.3:n.*157del
NM_000565.3:c.*157del NP_000556.1:n.*157del
NM_181359.2:c.*372del NP_852004.1:n.*372del
XM_005245139.1:c.*245del XP_005245196.1:n.*245del
XM_005245140.1:c.*405del XP_005245197.1:n.*405del
XM_006711298.1:c.*157del XP_006711361.1:n.*157del
XM_005245139.2:c.*245del XP_005245196.1:n.*245del
XM_005245140.3:c.*405del XP_005245197.1:n.*405del
XM_006711298.2:c.*157del XP_006711361.1:n.*157del
XM_017001199.2:c.*157del XP_016856688.1:n.*157del
XM_017001200.2:c.*157del XP_016856689.1:n.*157del
XM_017001201.2:c.*405del XP_016856690.1:n.*405del
NM_000565.4:c.*157del MANE Select NP_000556.1:n.*157del
NM_181359.3:c.*372del NP_852004.1:n.*372del
NM_001382769.1:c.*157del NP_001369698.1:n.*157del
NM_001382770.1:c.*157del NP_001369699.1:n.*157del
NM_001382771.1:c.*157del NP_001369700.1:n.*157del
NM_001382772.1:c.*157del NP_001369701.1:n.*157del
NM_001382773.1:c.*372del NP_001369702.1:n.*372del
NM_001382774.1:c.*157del NP_001369703.1:n.*157del